論文

査読有り
2017年3月1日

Fluid shear stress applied by orbital shaking induces MG-63 osteosarcoma cells to activate ERK in two phases through distinct signaling pathways

Biochemistry and Biophysics Reports
  • Takashi Fukada
  • ,
  • Hiroki Sakajiri
  • ,
  • Mito Kuroda
  • ,
  • Noriyuki Kioka
  • ,
  • Kenji Sugimoto

9
開始ページ
257
終了ページ
265
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bbrep.2017.01.004
出版者・発行元
Elsevier B.V.

Fluid shear stress (FSS) induces a series of biochemical responses in osteoblasts, and this “mechanoresponse” regulates their survival, proliferation and differentiation. However, the events in cells immediately after FSS application are unclear, and how biochemical signals from soluble factors modify the mechanoresponses is largely unknown. We used the orbital shaking method, instead of the frequently used parallel plate method, to examine activation of ERK and AKT by FSS for detailed tracking of its temporal transition. We found that ERK activation by orbital shaking was biphasic. The early phase was independent of Ca2+, PI3-kinase, and Rho kinase but required RAF activity. The late phase was dependent on Ca2+ but not RAF. These results suggest that the superior time-resolving capability of the orbital shaking method to separate the previously unrecognized Ca2+-independent early phase of ERK activation from the late phase. We also found that a certain combination of serum starvation and medium renewal affected ERK activation by FSS, suggesting that a soluble factor(s) may be secreted during serum starvation, which modified the phosphorylation level of ERK. These findings revealed novel aspects of the osteoblastic mechanoresponses and indicated that the orbital shaking method would be a useful, complementary alternative to the parallel plate method for certain types of study on cellular mechanoresponses.

リンク情報
DOI
https://doi.org/10.1016/j.bbrep.2017.01.004
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28956013
ID情報
  • DOI : 10.1016/j.bbrep.2017.01.004
  • ISSN : 2405-5808
  • PubMed ID : 28956013
  • SCOPUS ID : 85009834492

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